NCK2 and amyotrophic lateral sclerosis: Results from this cohort showed incidence of novel FTO and TBC1D1 genetic variants associated with Amyotrophic lateral sclerosis (ALS) in the Greek population [64], or six genomic variants (SLC9A4 c.1919G>A, KIAA1109 c.2933T>C and c.4268_4269delCCinsTA, HoxB6 c.668C>A, HoxD12 c.418G>A, and NCK2 c.745_746delAAinsG) with the potential of celiac disease predisposition in the Greek population [65].